Colorectal Cancer Clinical Trial
Official title:
Screening for Stomach Diseases and Colorectal Neoplasms With the Fecal Testing: a Population-based Randomized Study
1. The abundant results from this trial will be helpful for assessing the feasibility of
increasing stool sampling and shortening screening interval in population setting for
lower and upper gastrointestinal tract lesions, their long-term effects, and the
respective cost-effectiveness.
2. The study will evaluate the value of population-based screen and treatment for H. pylori
infection when the HPSA is combined with the FIT.
Growing body of evidences have shown that fecal immunochemical test (FIT) outperform guaiac
fecal occult blood test (gFOBT) in terms of sensitivity, neoplasm detection rate and public
participation. Though direct outcome evidence is still lacking for FIT, it is anticipated to
have higher colorectal cancer (CRC) mortality and incidence reduction compared with gFOBT. In
Taiwan, nation-wide CRC screening program has been launched since the year of 2004 ,which
provides biennial FIT screening for adults aged 50 to 69 years. Currently available data from
the Bureau of Health Promotion has shown a significant stage-shift effect, an early indicator
of screening effectiveness, by this screening program.
Nevertheless, the aforementioned advantages of FIT, missed neoplasms and interval cancer
still exists under the current one-day stool sampling method with biennial screening
interval, which might affect the effectiveness of overall screening program. Increase the
number of stool samples or shortening of screening interval may be helpful for early
detection of clinically significant neoplasms but it remains unclear whether such an approach
may lower the screenee compliance or public participation. Moreover, its impact on the demand
of confirmatory colonoscopy and cost-effectiveness of the whole screening program is still
largely unknown and need to be further investigated.
In this study, we firstly aim to randomly allocate screening attendee to one of the following
four arms: one-day sampling with annual screening, one-day sampling with biennial screening,
two-day sampling with annual screening, and two-day sampling with biennial screening.
Participation rate, positive rates of FIT, detection rate for neoplasms, positive predictive
value, and long-term outcome including cancer incidence and mortality will be calculated and
compared among four groups.
Secondly, in the Taiwanese population, which is a typical presentation of Asian populations,
although the incidence of colorectal cancer is rapidly increasing, Helicobacter
pylori-related upper gastrointestinal pathologies remain highly prevalent, which may imply
that mass screening solely based on FIT could be insufficient as significant upper GI
pathologies can be missed. Since the FIT does not predict upper GI pathologies, the adjunct
of an「Helicobacter pylori stool-antigen test (HpSA) 」 may be a potential candidate to realize
a pan-detecting assay based on stool samples in a population in which both lower and upper GI
lesions are equally prevalent. Therefore, in the present study, we will also evaluate the
value of simultaneous FIT and HpSA test in the community-based mass screening. We invited
subjects in a randomized study to receive the FIT or the FIT plus HPSA. Those who are tested
positive for HPSA will receive upper endoscopic examination and anti-H. pylori treatment. For
the short-term indicators, we will evaluate the participation rate and diagnostic yield when
the HPSA is added. For the long-term indicators, we will compare the incidence and mortality
of gastric cancer as well as complicated peptic ulcers.
To summary, this study includes two randomized trials:
1. To make a comparison between one-day sampling with annual screening, one-day sampling
with biennial screening, two-day sampling with annual screening, and two-day sampling
with biennial screening using FIT;
2. To make a comparison between FIT plus HpSA and FIT alone for screening.
Finally, the cost-effectiveness analysis will be also conducted using previously established
Markov model of CRC natural history and stomach diseases (such as dyspepsia, peptic ulcer
disease, and gastric cancer) using the results ascertained from this trial.
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